Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721952Generated: October 27, 2026

2-Methylvaleric acid → N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-methylpentanoyl)thiourea

https://huagongshe.com/reaction/721952

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylvaleric acidHCID 7341—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methylvaleryl chlorideHCID 107385—
Reactant3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
Reactant2-Methylpentanoyl isothiocyanateHCID 21890479—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-methylpentanoyl)thioureaHCID 2189102794%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 2-methylpentanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 2-methylpentanoyl isothiocyanate was prepared using the resultant 2-methylpentanoyl chloride as a starting compound according to the description of the literature. The resultant 2-methylpentanoyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]aniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 16 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (69 mg, yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-e525d58f1bd44e74be3ea4546b6b9ba2
Source noteuspto-grants-2006_11